Principal, Global Feasibility – Sponsor-dedicated

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Capable of independently managing the most complex RFPs and Feasibility objectives across all therapeutic domains;

• Actively collaborates with Business Units, Business Development, Medical Directors, Business Analysts, and other team members as necessary to evaluate RFP challenges and works together towards solutions with no oversight required.

• Proactively seeks solutions for non-standard requests.

• Serves as the representative of Global Feasibility in all interactions with both internal and external stakeholders, demonstrating the utmost collaboration, professionalism, integrity, and quality.

• Possesses the ability to operate efficiently within established processes and manage an average to high number of assignments and complexities concurrently across all therapeutic areas as required.

• Responsible for the development, analysis, and delivery of pre-award site-level feasibility assessments in the form of presentations and/or written reports for both internal and external stakeholders, independently.

• Maintains the highest standards within the Global Feasibility role;

• Exhibits excellent editing-level verbal, written, and visual communication skills.

• Independently aids in the preparation of materials for and attends bid defense teleconferences and meetings, with minimal review and supervision from a line manager or delegate.

• May oversee the work of other team members as necessary on larger collaborative projects, multi-study assignments, or alliance/FSP partnerships.

• Capable of mentoring junior team members up to the Senior Feasibility Lead, Global Feasibility level, providing guidance on text and slide deck editing, as well as data collection and processing insights across all therapeutic indications.

• May engage in and support activities pertaining to department staff operations.

⛳️ Requirements

• BS / RN / MS with 7 years of relevant experience or

• PhD / MD with 3 years of relevant experience

• Comprehensive knowledge of drug development, including a thorough understanding of the processes related to global country and site feasibility, clinical study start-up, and business operations.

• Experience in clinical research encompassing clinical trial conduct, knowledge of GCP, and a solid understanding of the processes linked to study/project management, monitoring, clinical, and regulatory operations.

• Proven track record of success in a customer service role, demonstrating the ability to meet customer expectations.

• Strong verbal and written communication capabilities.

• Effective presentation and facilitation skills.

• Well-honed strategic planning, observational, analytical operational execution, and problem-solving abilities.

• Robust business consultancy skills, including the capacity to persuade, negotiate, and mediate conflict.

• Ability to multitask under tight deadlines across various projects with specific and unique requirements, while maintaining attention to detail and high-quality work.

• Competent in synthesizing key messages derived from multiple data sets.

🏝️ Benefits

• We are dedicated to the development of our people through career growth and advancement;

• Supportive and engaged line management;

• Technical and therapeutic area training;

• Peer recognition and a total rewards program.

• We are committed to fostering an inclusive culture – where you can genuinely be yourself.